Label: LIQUID CALLUS REMOVER- salicylic acid liquid
- NDC Code(s): 56104-501-00
- Packager: Premier Brands of America Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 14, 2024
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- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only.
Do not use
- on irritated skin
- on any area that is infected or reddened
- if you are a diabetic or if you have poor blood circulation
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Directions
- wash the affected area and dry thoroughly
- apply one drop at a time with applicator to sufficiently cover each corn/callus
- let dry
- repeat this procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)
- may soak corn/callus in warm water for 5 minutes to assist in removal
- Other information
- Inactive ingredients
- Questions?
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INGREDIENTS AND APPEARANCE
LIQUID CALLUS REMOVER
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:56104-501 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 170 mg in 1 mL Inactive Ingredients Ingredient Name Strength CAMPHOR (NATURAL) (UNII: N20HL7Q941) CASTOR OIL (UNII: D5340Y2I9G) PYROXYLIN (UNII: KYR8BR2X6O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:56104-501-00 1 in 1 CARTON 09/11/2023 1 9.8 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M030 09/11/2023 Labeler - Premier Brands of America Inc. (063849780)